Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report

Fanconi syndrome is one of the primary renal manifestations of mitochondrial cytopathies caused by mitochondrial DNA (mtDNA) mutation. The common 4977-bp mtDNA deletion has been reported to be associated with aging and diseases involving multiple extrarenal organs. Cases of Fanconi syndrome caused b...

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Detalles Bibliográficos
Autores principales: Li, Ting, Lu, Zhihong, Wang, Jingjing, Chen, Junyi, Fu, Haidong, Mao, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535084/
https://www.ncbi.nlm.nih.gov/pubmed/34682152
http://dx.doi.org/10.3390/children8100887

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535084/
https://www.ncbi.nlm.nih.gov/pubmed/34682152
http://dx.doi.org/10.3390/children8100887

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